Title of article
A New Intra-Arterial DeliveryPlatform for Pro-Arteriogenic Compounds to Stimulate Collateral Artery Growth Via Transforming Growth Factor-β1 Release Original Research Article
Author/Authors
Sebastian Grundmann، نويسنده , , Niels van Royen، نويسنده , , Gerard Pasterkamp، نويسنده , , Nieves Gonzalez، نويسنده , , Edze J. Tijsma، نويسنده , , Jan J. Piek، نويسنده , , Imo E. Hoefer، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
8
From page
351
To page
358
Abstract
Objectives
The purpose of this study was to develop a cytokine-eluting stent to stimulate collateral artery growth (arteriogenesis) in the peripheral circulation of the rabbit via local transforming growth factor (TGF)-β1 release.
Background
The stimulation of arteriogenesis with cytokines is a potential new treatment option for patients suffering from vascular occlusive diseases. However, the lack of a delivery platform for continuous intra-arterial application of pro-arteriogenic compounds has hampered the clinical implementation of this promising therapeutic strategy.
Methods
Different polymer coatings were tested regarding their suitability for cytokine release. Fifty-four rabbits underwent implantation of bare-metal stents (BMS), polymer-only coated stents (PDLLA), polymer-coated TGF-β1–eluting stents (TGF) in the iliac artery, or bolus infusion of TGF-β1 and subsequent femoral artery ligation. Collateral artery growth was assessed with fluorescent microspheres, angiography, and histological quantification of the proliferation marker Ki67. In-stent neointima formation was measured in histological sections of plastic-embedded stents.
Results
A TGF-β1–loaded coating based on poly(D,L-lactide) released up to 2.4 μg active TGF-β1 over a period of 24 h. Perfusion measurements revealed a significant increase in collateral conductance after TGF-β1 stent implantation compared with the control groups ([ml/min/100 mm Hg] BMS: 47.8 ± 2.5; PDLLA: 44.1 ± 3.9; TGF: 91.3 ± 32.6). Bolus infusion of TGF-β1 had no effect. Collateral arteries showed a higher proliferation activity in the TGF-treated group. At 7 days, no significant difference in in-stent neointima formation was observed.
Conclusions
We first describe the use of a cytokine-releasing stent to stimulate collateral artery growth. These results show that intra-arterial cytokine-releasing devices might serve as a novel platform for the delivery of compounds affecting biological processes downstream of the site of implantation.
Keywords
BMS , vascular endothelial growth factor , VEGF , ELISA , Molecular weight , vascular smooth muscle cells , Fibroblast growth factor , MMA , PbS , PDLLA , Mw , VSMC , HE , HUVECs , FGF , bare-metal stent(s) , phosphate buffered saline , enzyme linked immunosorbent assay , hematoxyline and eosine , human umbilical endothelial cells , methyl-methacrylate , PBMA , poly(n-butyl methacrylate) , poly(D , L-lactide) , PEVA , poly(ethylene-co-vinyl acetate) , rhTGF-?1 , recombinant human transforming growth factor ?1
Journal title
JACC (Journal of the American College of Cardiology)
Serial Year
2007
Journal title
JACC (Journal of the American College of Cardiology)
Record number
472677
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